Európai Unió - litván - EMA (European Medicines Agency)

roche registration gmbh  - entrectinib - cancer; carcinoma, non-small-cell lung - antinavikiniai vaistai - rozlytrek as monotherapy is indicated for the treatment of adult and paediatric patients 12 years of age and older with solid tumours expressing a neurotrophic tyrosine receptor kinase (ntrk) gene fusion,who have a disease that is locally advanced, metastatic or where surgical resection is likely to result in severe morbidity, andwho have not received a prior ntrk inhibitorwho have no satisfactory treatment options. rozlytrek as monotherapy is indicated for the treatment of adult patients with ros1 positive, advanced non small cell lung cancer (nsclc) not previously treated with ros1 inhibitors.

Litvánia - litván - SMCA (Valstybinė vaistų kontrolės tarnyba)

accord healthcare b.v. - klozapinas - tabletės - 25 mg - clozapine

Litvánia - litván - SMCA (Valstybinė vaistų kontrolės tarnyba)

accord healthcare b.v. - klozapinas - tabletės - 100 mg - clozapine

Európai Unió - litván - EMA (European Medicines Agency)

pfizer europe ma eeig - nirmatrelvir, ritonavir - covid-19 virus infection - paxlovid is indicated for the treatment of coronavirus disease 2019 (covid-19) in adults who do not require supplemental oxygen and who are at increased risk for progressing to severe covid 19.

Európai Unió - litván - EMA (European Medicines Agency)

novartis europharm limited - asciminib hydrochloride - leukemija, mielogeninė, lėtinė, bcr-abl teigiama - antinavikiniai vaistai - scemblix is indicated for the treatment of adult patients with philadelphia chromosome positive chronic myeloid leukaemia in chronic phase (ph+ cml cp) previously treated with two or more tyrosine kinase inhibitors (see section 5.

Európai Unió - litván - EMA (European Medicines Agency)

mylan pharmaceuticals limited - teriflunomide - išsėtinė sklerozė, grįžtamoji-pervedimo - imunosupresantai - teriflunomide mylan is indicated for the treatment of adult patients and paediatric patients aged 10 years and older (body weight > 40 kg) with relapsing remitting multiple sclerosis (ms) (please refer to section 5. 1 of the smpc for important information on the population for which efficacy has been established).

Európai Unió - litván - EMA (European Medicines Agency)

accord healthcare s.l.u. - teriflunomide - išsėtinė sklerozė, grįžtamoji-pervedimo - imunosupresantais, pasirinktinio imunosupresantais - teriflunomide accord is indicated for the treatment of adult patients and paediatric patients aged 10 years and older with relapsing remitting multiple sclerosis (ms) (please refer to section 5. 1 for important information on the population for which efficacy has been established).

Litvánia - litván - SMCA (Valstybinė vaistų kontrolės tarnyba)

stada arzneimittel ag - teriflunomidas - plėvele dengtos tabletės - 14 mg - teriflunomide

Litvánia - litván - SMCA (Valstybinė vaistų kontrolės tarnyba)

krka, d.d., novo mesto - teriflunomidas - plėvele dengtos tabletės - 14 mg - teriflunomide

Litvánia - litván - SMCA (Valstybinė vaistų kontrolės tarnyba)

egis pharmaceuticals plc - teriflunomidas - plėvele dengtos tabletės - 14 mg - teriflunomide